Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2239547 0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs1042779 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 4
rs2271893 0.925 0.040 2 96739703 intron variant G/A snv 0.23 3